A comprehensive, end-to-end service from concept through to manufacturing— with full documentation and ISO compliance at every stage.
Let us develop and complete an audit-ready folder alongside your project.
The last 5% of any project is the hardest — we see it through.
We can make complete product on site, or transfer to and train your preferred OEM manufacturer.
From early-stage assay research through to large-scale manufacturing, we offer specialist support at every point in the lateral flow development lifecycle.
Research, materials discovery and full development under ISO 13485.
In-house and collaborative design and manufacture of key proteins.
Side-by-side modernisation of current products for improved performance.
High-quality assay components manufactured for third-party use.
Clear, unambiguous access to your project development phases and data.
Proprietary technology in the manufacture and labelling of coloured gold particles.
Sensitivity upgrades and dynamic range manipulation for existing assays.
Project management of quality moulding and production instrumentation.
From initial screening to validated, production-ready performance.
Every batch undergoes rigorous post-production verification against defined release criteria, ensuring full traceability, batch consistency, and compliance before any component leaves our facility.
Dedicated production teams follow validated SOPs through every step of device assembly — from cassette loading and desiccant integration to final packaging — maintaining product integrity at scale.
We are a highly focused development and manufacturing company. Our average experience per head in the medical assay development laboratory is 12 years — depth that translates directly into project success.
Managing Director · New Development
Managing Director · New Development
Nick moved from pharmaceutical manufacture into medical diagnostics and has worked specifically in lateral flow IVD development for 25 years, with companies including Abbott Diagnostics, Alere, BBI and Vision Biotech.
Laboratory Manager
Laboratory Manager
An analytical chemist with advanced post-graduate qualifications in Operations Management and Quality. Julianne has 12 years of IVD experience, has developed a significant number of new assays, and controls all laboratory manufacturing operations at LFL.
Laboratory Manufacturing & QC
Laboratory Manufacturing & QC
Yumna brings a strong background in Microbiology and QA. She has contributed to multiple development projects and guided LFL through several regulatory audits with her QA expertise.
Laboratory Manufacturing & QC
Laboratory Manufacturing & QC
Jenna has developed excellent laboratory and manufacturing credentials. She holds a B.Sc from Stellenbosch University and is an invaluable member of the development team.
Operations
Operations
Greg brings many years of quality laboratory experience and currently manages all operational functions at LFL, including overseeing the company's non-laboratory staff.
Quality Assurance
Quality Assurance
Originally an analytical chemist, Roslyn completed an MBA before moving into Quality Management. She has worked and managed quality sites at some of South Africa's largest companies.
Line Supervisors
Line Supervisors
Faeza Williams, Caren da Silva and Cynthia Philander have each worked in IVD manufacturing for over 15 years, bringing deep supervisory expertise to our assembly, stores and packaging functions.
Accounts
Accounts
Wendy manages our debtors and creditors, orders, all financial queries and tax compliance. She has an extensive track record in small and medium enterprise accountancy.
If you are looking for a specialist lateral flow development house with high transparency and cost efficiencies versus our competitors, then let's talk — you may be surprised.